Evidence map›Paper›PMID 17031666›Full record

ArticlePflugers Archiv : European journal of physiology2007

Evidence that TRPC4 supports the calcium selective I(CRAC)-like current in human gingival keratinocytes.

Sahba Fatherazi, Richard B Presland, Carol M Belton, Paul Goodwin, Montaser Al-Qutub, Zorica Trbic, Glen Macdonald, Mark M Schubert, Kenneth T Izutsu

Abstract read
PubMed Publisher
In one paragraph

Article in Pflugers Archiv : European journal of physiology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
0.7field-weighted citation impact, top 36% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Wound Repair and CaCells · 2024
    Review
  2. The Molecular Heterogeneity of Store-Operated CaInternational journal of molecular sciences · 2023
    Review
  3. Article
  4. Article
  5. Store-operated calcium channels in skin.Frontiers in physiology · 2022
    Review
  6. Role of Store-Operated CaBiomolecules · 2021
    Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Possible antagonistic effects of the TRPC4 channel blocker ML204 on MThe Journal of veterinary medical science · 2018
    Article
  12. Skin Barrier and Calcium.Annals of dermatology · 2018
    Review
  13. Review
  14. Review
  15. TRP channels in the skin.British journal of pharmacology · 2014
    Review
  16. ORAI1 calcium channel orchestrates skin homeostasis.Proceedings of the National Academy of Sciences of the United States of America · 2013
    Article
  17. Kv7/M-type potassium channels in rat skin keratinocytes.Pflugers Archiv : European journal of physiology · 2013
    Article
  18. Role of the calcium-sensing receptor in calcium regulation of epidermal differentiation and function.Best practice & research. Clinical endocrinology & metabolism · 2013
    Review
  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 1 institution in 1 country.

Sahba FatheraziDepartment of Oral Biology, University of Washington, Seattle, WA 98195-7132, USA. fats@u.washington.edu
Richard B Presland
Carol M Belton
Paul Goodwin
Montaser Al-Qutub
Zorica Trbic
Glen Macdonald
Mark M Schubert
Kenneth T Izutsu
University of Washington · US

Funding

CAPACITATIVE CALCIUM ENTRY AND STORES IN KERATINOCYTESR01AR046254 · NIAMS · UNIVERSITY OF WASHINGTON · PI IZUTSU, KENNETH T · 2000 to 2002
$774k
NIAMS NIH HHS R01 AR046254
6 · The paper itself

Abstract

We previously demonstrated that high external [Ca(2+)] activated two Ca(2+) currents in human gingival keratinocytes (HGKs): an initial small I(CRAC)-like current and a second large nonspecific cation current (Fatherazi S, Belton CM, Cai S, Zarif S, Goodwin PC, Lamont RJ, Izutsu KT; Pflugers Arch 448:93-104, 2004). It was recently shown that TRPC1, a member of the transient receptor potential protein family, is a component of the store-operated calcium entry mechanism in keratinocytes. To further elucidate the molecular identity of these channels, we investigated the expression of TRPC4 in gingival tissue and in cultured keratinocytes, and the effect of knockdown of TRPC4 expression on the Ca(2+) currents and influx. Immunohistochemistry showed TRPC4 was present in gingival epithelium as well as in HGKs cultured in different [Ca(2+)]s. Results from tissue and cultured HGKs demonstrated TRPC4 expression decreased with differentiation. Knockdown of TRPC4 in proliferating HGKs with antisense oligonucleotides significantly reduced the intracellular [Ca(2+)] increase obtained upon exposure to high external [Ca(2+)]. Antisense knockdown of TRPC4 expression was confirmed by reverse transcriptase polymerase chain reaction, Western blot, and immunofluorescence microscopy of transfected HGKs. Immunofluorescence microscopy and patch clamp measurements in Lucifer-yellow-tagged, antisense-treated HGKs showed attenuation of TRPC4 expression levels as well as attenuation of the I(CRAC)-like current in the same cell, whereas the large nonspecific cation current was unchanged but significantly delayed. Cells transfected with a scrambled TRPC4 oligonucleotide showed no change in either the I(CRAC)-like or nonspecific currents. The results indicate that TRPC4 is an important component of the I(CRAC)-like channel in HGKs.

Indexed as

CalciumCells, CulturedFluorescent DyesGingivaHumansIsoquinolinesKeratinocytesMembrane PotentialsOligonucleotides, AntisensePatch-Clamp TechniquesRNA, MessengerTransfectionTRPC Cation ChannelsCalciumFluorescent DyesIsoquinolineslucifer yellowOligonucleotides, AntisenseRNA, MessengerTRPC4 ion channelTRPC Cation Channels

Identifiers

PMID17031666
OpenAlexW2056276104

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.